Comparison of Cervical and TMJ Parameters in Young Adults With and Without Text Neck Syndrome
Comparison of Physical Parameters Related to the Cervical Region and Temporomandibular Joint in Young Individuals With and Without Text Neck Syndrome: A Cross-Sectional Study
The aim of this cross-sectional study is to compare temporomandibular joint (TMJ) and cervical spine parameters between young university students aged 18-30 years with and without text neck syndrome, a modern overuse condition caused by prolonged digital device use and repetitive forward head flexion. Given the anatomical, biomechanical, and functional connections between the stomatognathic system and the cervical region, prolonged altered posture may contribute to TMJ dysfunction, pain, and altered physical metrics. Participants are categorized into two groups based on photographic and self-reported text neck severity (levels 3-4 for text neck vs. levels 1-2 for non-text neck) and evaluated across multiple physical parameters, including craniovertebral and cervicothoracic angles, active cervical and mandibular range of motion, cervical joint position sense, neck and TMJ pain intensity via Visual Analog Scale, TMJ dysfunction severity using the Turkish-validated Fonseca Questionnaire, static balance via the single-leg stance test, and dynamic balance via the Y Balance Test.
Aperçu de l'étude
Statut
Type d'étude
Inscription (Estimé)
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
The study population consists of young adult university students aged 18 to 30 years recruited from a university campus environment. Participants will be sampled from healthy undergraduate and graduate students who routinely use digital devices (such as smartphones and tablets) in their daily academic and personal activities.
La description
Inclusion Criteria:
- University students aged between 18 and 24 years,
- Group 1: Individuals with level 3 or level 4 text neck posture based on the self-reported posture assessment diagram,
- Group 2: Individuals with level 1 or level 2 text neck posture based on the self-reported posture assessment diagram,
- Being physically and mentally eligible to participate in the study,
- Willingness to voluntarily participate and provide written informed consent prior to study enrollment.
Exclusion Criteria:
- History of cervical spine surgery,
- Ongoing orthodontic treatment,
- Receiving medical treatment related to the neck or jaw region within the last 3 months,
- Exposure to trauma related to the neck or jaw region within the last 3 months,
- Presence of a diagnosed psychiatric disorder.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Modèles d'observation: COHORT
- Perspectives temporelles: CROSS_SECTIONAL
Cohortes et interventions
Groupe / Cohorte |
|---|
|
Text Neck Syndrome Group
|
|
Non-Text Neck Group
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Cervical Posture Angles
Délai: Baseline (at a single assessment point)
|
Baseline (at a single assessment point)
|
|
|
Cervical and Temporomandibular Joint Pain Intensity
Délai: Baseline (at a single assessment point).
|
Description: Will be evaluated using a 10-cm Visual Analog Scale (VAS; 0 = no pain, 10 = worst imaginable pain) for neck pain and TMJ pain (at rest, during activity, and while chewing). |
Baseline (at a single assessment point).
|
|
Cervical Range of Motion (CROM)
Délai: Baseline (at a single assessment point).
|
Description: Will be evaluated in degrees for active cervical flexion, extension, bilateral lateral flexion, and bilateral rotation using the CROM (Cervical Range of Motion) device. |
Baseline (at a single assessment point).
|
|
Mandibular Range of Motion
Délai: Baseline (at a single assessment point).
|
Description: Will be measured in millimeters (mm) using a digital caliper and ruler for maximum mouth opening, right/left lateral movements, and protrusion. |
Baseline (at a single assessment point).
|
|
Text Neck Posture Classification
Délai: Baseline (at a single assessment point).
|
Text neck posture will be assessed using both self-reported perception and standardized photographic analysis. |
Baseline (at a single assessment point).
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Temporomandibular Joint Dysfunction Severity
Délai: Baseline.
|
Description: Will be evaluated using the Turkish-validated Fonseca Questionnaire (10 items, total score 0-100; higher scores indicate greater TMD severity). |
Baseline.
|
|
Cervical Joint Position Sense (JPS)
Délai: Baseline
|
Description: Will be evaluated in degrees using the CROM device across flexion-extension, lateral flexion, and rotation planes to measure absolute error from a target angle |
Baseline
|
|
Static Balance
Délai: Baseline.
|
Description: Will be measured in seconds with eyes open and eyes closed on a firm surface. |
Baseline.
|
|
Dynamic Balance Assessment using the Y Balance Test
Délai: Baseline
|
Baseline
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- E-60116787-020-622674
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .